The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway

Por Ciura, Sorana, Sellier, Chantal, Campanari, Maria-Letizia, Charlet-Berguerand, Nicolas, Kabashi, Edor
Publicado no Autophagy (2016)

Neuromuscular Junction Impairment in Amyotrophic Lateral Sclerosis: Reassessing the Role of Acetylcholinesterase

Por Campanari, Maria-Letizia, García-Ayllón, María-Salud, Ciura, Sorana, Sáez-Valero, Javier, Kabashi, Edor
Publicado no Front Mol Neurosci (2016)

Increased expression of readthrough acetylcholinesterase variants in the brains of Alzheimer's disease patients

Por Campanari, Maria-Letizia, Navarrete, Francisco, Ginsberg, Stephen D., Manzanares, Jorge, Sáez-Valero, Javier, García-Ayllón, María-Salud
Publicado no J Alzheimers Dis (2016)

CSF Presenilin-1 complexes are increased in Alzheimer’s disease

Por García-Ayllón, María-Salud, Campanari, María-Letizia, Brinkmalm, Gunnar, Rábano, Alberto, Alom, Jordi, Saura, Carlos A, Andreasen, Niels, Blennow, Kaj, Sáez-Valero, Javier
Publicado em 2013

Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death

Por Sellier, Chantal, Campanari, Maria‐Letizia, Julie Corbier, Camille, Gaucherot, Angeline, Kolb‐Cheynel, Isabelle, Oulad‐Abdelghani, Mustapha, Ruffenach, Frank, Page, Adeline, Ciura, Sorana, Kabashi, Edor, Charlet‐Berguerand, Nicolas
Publicado no EMBO J (2016)